ライフサイエンスコーパス: M. gallisepticum

1 11 days after experimental inoculation with M. gallisepticum.

2 upon direct contact of HD-11 cells with live M. gallisepticum.

3 ing the first genome-scale reconstruction of M. gallisepticum.

4 or transmission potential, among isolates of M. gallisepticum.

5 ce of naive juveniles or the introduction on M. gallisepticum.

6 ce increased rapidly after reintroduction of M. gallisepticum.

7 ucidate genomic variability among strains of M. gallisepticum.

8 he GAA repeats in M9/pMGA gene expression in M. gallisepticum.

9 antiserum recognizes a 150-kDa protein from M. gallisepticum.

10 promoterless lacZ gene and transformed into M. gallisepticum by using transposon Tn4001 as a vector.

11 inate catabolism and all genes examined from M. gallisepticum, C. perfringens, and S. pneumoniae were

12 M. gallisepticum cgMLST represents a standardized, accur

13 5 countries on 4 continents were typed using M. gallisepticum cgMLST.

14 Southern analysis of M. gallisepticum chromosomal DNA confirmed that the phas

15 A total of 425 M. gallisepticum conserved genes (49.85% of M. gallisept

16 For the transformants of M. gallisepticum containing the reporter with deletion o

17 ate that both GapA and CrmA are required for M. gallisepticum cytadherence and pathogenesis.

18 hat CrmA might play an essential role in the M. gallisepticum cytadherence process.

19 gment was used to probe a genomic library of M. gallisepticum DNA.

20 ast isolates of the pathogen collected after M. gallisepticum established itself in western North Ame

21 han proteins important for cytadherence, few M. gallisepticum factors or pathways contributing to hos

22 M permits the comprehensive screening of the M. gallisepticum genome for the identification of novel

23 M. gallisepticum conserved genes (49.85% of M. gallisepticum genome) were selected as core genome ta

24 ces obtained in this manner to the annotated M. gallisepticum genome, the precise locations of transp

25 A total of 81 M. gallisepticum genomes from 5 countries on 4 continent

26 t of this scheme, a diverse collection of 37 M. gallisepticum genomes was used to identify cgMLST tar

27 e novel insights into inter- and intrastrain M. gallisepticum genomic variability and the genetic bas

28 House finch-associated M. gallisepticum (HFMG) spread rapidly and increased in

29 MGA_1199, the M. gallisepticum homologue of the cytadherence-associate

30 rom Mycoplasma pneumoniae, and MGA_0928, the M. gallisepticum homologue of the M. pneumoniae cytoskel

31 re thought to be important for mechanisms of M. gallisepticum-host interaction, pathogenesis, and imm

32 ible that glycerol metabolism is required by M. gallisepticum in a niche that we have yet to study.

33 gallisepticum vaccines, and the detection of M. gallisepticum in game and free-flying song birds has

34 for disease manifestations characteristic of M. gallisepticum infection.

35 the second hypothesis that reintroduction of M. gallisepticum into a multiage group of previously exp

36 house finches and that the reintroduction of M. gallisepticum is sufficient to cause a new outbreak,

37 eproducible method for differentiation among M. gallisepticum isolates.

38 Comparative transcriptomic analysis of the M. gallisepticum live attenuated vaccine strain F and th

39 Global M. gallisepticum mutagenesis is currently limited to the

40 the experimentally determined growth rate of M. gallisepticum of 0.244+/-0.03[Formula: see text].

41 of M. synoviae, but not on the sialidase of M. gallisepticum or the sialidases or other enzymes esse

42 The reemergence of M. gallisepticum outbreaks among poultry, the increased

43 Moreover, molecular epidemiology of M. gallisepticum outbreaks can be performed using RFLP a

44 This construct was transformed into M. gallisepticum PG31.

45 criptomic vlhA gene expression directly from M. gallisepticum populations present on tracheal mucosae

46 ons in the natural host compared to virulent M. gallisepticum R(low).

47 These results indicate that M. gallisepticum regulates gene expression upon exposure

48 d from tracheas of 20 chickens infected with M. gallisepticum Rlow and 20 mock-infected animals at da

49 Fibronectin was found to be present in M. gallisepticum Rlow protein extracts by Western blotti

50 ng and the sequenced genomes compared to the M. gallisepticum Rlow reference genome.

51 nucleotide identity with the pMGA1.1 gene of M. gallisepticum S6.

52 first description of a functional gene from M. gallisepticum showing homology to cytadhesin genes fr

53 was to determine the feasibility of using an M. gallisepticum-specific gene encoding a phase-variable

54 rations, and significantly higher numbers of M. gallisepticum-specific IgG- and IgA-secreting plasma/

55 Currently, M. gallisepticum strain differentiation based on sequenc

56 enomic sequence of the virulent, low-passage M. gallisepticum strain R (R(low)) has been reported, ge

57 ed to investigate transcriptional changes in M. gallisepticum strain R(low) upon exposure to eukaryot

58 tion following challenge with the pathogenic M. gallisepticum strain R(low).

59 ltilocus sequence typing (cgMLST) scheme for M. gallisepticum strains and field isolates.

60 er of cgMLST allowed differentiation between M. gallisepticum strains of the same outbreak.

61 adults can initiate an epidemic and transmit M. gallisepticum to naive house finches and that the rei

62 designed to target 5 sequences unique to the M. gallisepticum ts-11 strain: vlhA3.04a, vlhA3.04b, vlh

63 3.05, and mg0359 was able to distinguish the M. gallisepticum ts-11 vaccine strain from field isolate

64 hypothetical protein gene, mg0359, unique to M. gallisepticum ts-11 vaccine strain.

65 Analyses of the genome of the M. gallisepticum vaccine strain F revealed numerous diff

66 eld isolates, whole-genome sequencing of the M. gallisepticum vaccine strain ts-11 and several "ts-11

67 A live attenuated M. gallisepticum vaccine strain, GT5, was previously sho

68 nt current approaches to quickly distinguish M. gallisepticum vaccine strains from field isolates.

69 aks among poultry, the increased use of live M. gallisepticum vaccines, and the detection of M. galli

70 in an attenuated strain and plays a role in M. gallisepticum virulence.

71 genomic variability and the genetic basis of M. gallisepticum virulence.

72 d reproducible methods for comparisons among M. gallisepticum whole genomes.

73 We recently reported that the interaction of M. gallisepticum with chicken tracheal epithelial cells

74 t the notion that the initial interaction of M. gallisepticum with host respiratory epithelial cells